ethyl 6-methylsalicylate

CCOC(=O)c1c(C)cccc1OC
Reaction #9038
ethyl 2-methoxy-6-methylbenzoate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1c(O)cccc1CBr
Reaction #257381
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1c(C)cccc1OC
Reaction #292402
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1c(C)cccc1Oc1ccnc2cc(OC)c(OC)cc12
Reaction #315807
title compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cccc(O)c1C(=O)O
Reaction #398240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1c(O)ccc(Br)c1C
Reaction #453136
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCOC(=O)c1c(C)cccc1OCCO[C@@H]1CCC[C@H](OCc2nc(-c3cccc(C)c3)oc2C)C1
Reaction #640752
Ethyl (1R,3S)-2-methyl-6-{2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxy]ethoxy}benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CC(=O)c1c(C)cccc1O
Reaction #678228
ketone
Ausbeute 72.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1cccc(O)c1C(=O)O
Reaction #749026
2-hydroxy-6-methylbenzoic acid
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCOC(=O)c1c(C)cccc1Oc1ccnc2cc(OC)c(OC)cc12
Reaction #773114
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)c1c(C)cccc1OC
Reaction #1245066
ethyl 2-methoxy-6-methylbenzoate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CCOC(=O)c1c(C)cccc1O[Si](C)(C)C(C)(C)C
Reaction #1311421
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCOC(=O)c1c(C)cccc1O[Si](C)(C)C(C)(C)C
Reaction #1329275
2-(tert-butyl-dimethyl-silanyloxy)-6-methyl-benzoic acid ethyl ester
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
C=CCOc1cccc(C)c1C(=O)O
Reaction #1346150
2-Allyloxy-6-methyl-benzoic acid
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
CCOC(=O)c1c(C)cccc1OC
Reaction #1669462
ethyl 2-methoxy-6-methylbenzoate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_05
Cc1cccc(O)c1C(=O)O
Reaction #1898206
2-hydroxy-6-methylbenzoic acid
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
CCOC(=O)c1c(C)cccc1O[Si](C)(C)C(C)(C)C
Reaction #2275196
2-(tert-butyl-dimethyl-silanyloxy)-6-methyl-benzoic acid ethyl ester
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_06
CCOC(=O)c1c(O)cccc1CBr
Reaction #2339024
2-bromomethyl-6-hydroxy-benzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_01
CCOC(=O)c1c(C)cccc1O
Reaction #2393311
title product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_08
CCOC(=O)c1c(C)cccc1OCCOC1CCCC(OCc2nc(-c3cccc(C)c3)oc2C)C1
Reaction #2427368
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)